NDC 50436-0752 Atenolol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50436 - Unit Dose Services
- 50436-0752 - Atenolol
Product Characteristics
Product Packages
NDC Code 50436-0752-3
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 50436-0752?
What are the uses for Atenolol?
Which are Atenolol UNII Codes?
The UNII codes for the active ingredients in this product are:
- ATENOLOL (UNII: 50VV3VW0TI)
- ATENOLOL (UNII: 50VV3VW0TI) (Active Moiety)
Which are Atenolol Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- POVIDONE K30 (UNII: U725QWY32X)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
What is the NDC to RxNorm Crosswalk for Atenolol?
- RxCUI: 197379 - atenolol 100 MG Oral Tablet
- RxCUI: 197381 - atenolol 50 MG Oral Tablet
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".